Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823917Generated: October 30, 2026

1-(Chloromethoxy)-2-methoxyethane → HCID 22147941, compound

https://huagongshe.com/reaction/1823917

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 178526495HCID 178526495—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22147941HCID 2214794146%

Reaction Steps

To a solution of 3-iodo-5-nitro-1H-indazole (10.0 g, 34.6 mmol) in THF (50 ml) was added sodium bis(trimethylsilyl)amide (1M in THF, 48.4 mmol, 48.4 ml) and the solution stirred at room temperature for 20 minutes. 2-methoxyethoxymethyl chloride (4.9 g, 39.1 mmol, 4.5 ml) was added and the solution stirred at room temperature for 15 hours. The reaction was quenched with ammonium chloride (30 ml, saturated aqueous) and extracted into ethyl acetate (3×50 ml). The combined organic extracts were dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by flash column chromatography on silica gel (1:1 EtOAc:hexanes) to give the title compound as an orange solid (6.0 g). 1H NMR (400 MHz, CDCl3) δ 3.35 (3H, s), 3.50–3.52 (2H, m), 3.68–3.70 (2H, m), 5.86 (1H, s), 7.69 (1H, d), 8.38 (1H, d), 8.53 (1H, s). MS (ES+) m/e=378.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041687B2
Source datasetuspto-grants-2006_05
ORD IDord-45e6f6e4960d4ace8d257b4bfe1b7418
Source noteuspto-grants-2006_05